Radiation therapy versus chemotherapy as initial treatment for localized nasal natural killer (NK)/T-cell lymphoma: a single institute survey in Taiwan

Background: To clarify the role of intention to treat for patients with localized nasal natural killer (NK)/T-cell lymphoma, and to determine the prognostic factors for these patients. Patients and methods: We conducted a retrospective review of 46 patients with localized nasal NK/T-cell lymphomas t...

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Published in:Annals of oncology Vol. 15; no. 4; pp. 618 - 625
Main Authors: You, J.-Y., Chi, K.-H., Yang, M.-H., Chen, C.-C., Ho, C.-H., Chau, W.-K., Hsu, H.-C., Gau, J.-P., Tzeng, C.-H., Liu, J.-H., Chen, P.-M., Chiou, T.-J.
Format: Journal Article
Language:English
Published: Oxford Oxford University Press 01-04-2004
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Summary:Background: To clarify the role of intention to treat for patients with localized nasal natural killer (NK)/T-cell lymphoma, and to determine the prognostic factors for these patients. Patients and methods: We conducted a retrospective review of 46 patients with localized nasal NK/T-cell lymphomas treated at a single institute between January 1988 and July 2002. Results: The type of intended treatment was a significant factor for overall survival (OS) (5-year OS: RT versus CT = 83.3% versus 28.6%, P = 0.0269) or failure-free survival (FFS) (5-year FFS: RT versus CT = 83.3% versus 27.1%, P = 0.0247). In the intended chemotherapy group, salvage with radiotherapy was superior to chemotherapy alone for OS (5-year OS: 42.2% versus 20.0%, P = 0.0252) or FFS (5-year FFS: 41.0% versus 20.0%, P = 0.0352). On multivariate analysis, both N stage and serum lactate hehydrogenase level were independent factors for OS and FFS. No radiotherapy was an independent adverse factor for OS; advanced T stage and more than one extranodal involvement were independent adverse factors for FFS. Conclusions: Patients with localized nasal NK/T-cell lymphomas were better managed with radiotherapy as front-line therapy. The advantage of radiotherapy persisted even as palliative therapy after chemotherapy.
Bibliography:ark:/67375/HXZ-D233Q017-B
istex:C0A6F1D856A8A27D6DABFA542A8D8D27F9C66394
local:mdh143
Received 1 December 2003; accepted 23 December 2003
ObjectType-Article-1
SourceType-Scholarly Journals-1
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ISSN:0923-7534
1569-8041
DOI:10.1093/annonc/mdh143